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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1906166생성일: 2026년 10월 24일

1,3-Butanedione, 1-(2-furanyl)- → 3-Amino-1-(2-furanyl)-2-buten-1-one

https://huagongshe.com/ko/reaction/1906166

반응식

참여 물질

역할이름HCID투입량
반응물1,3-Butanedione, 1-(2-furanyl)-HCID 12168—
반응물Ammonium AcetateHCID 517165—
용매TolueneHCID 1140—
생성물3-Amino-1-(2-furanyl)-2-buten-1-oneHCID 7044814548.9%

반응 단계

The intermediate 3-amino-1-(2-furanyl)-2-buten-1-one was prepared as follows: A mixture containing 165 g of 1-(2-furanyl)-1,3-butanedione, 700 ml of toluene and 200 g of ammonium acetate was azeotroped for six hours, cooled and concentrated to dryness in vacuo. The residue was dissolved in isopropyl alcohol, the solution treated with decolorizing charcoal and filtered, and the filtrate concentrated to remove the solvent. The remaining residue was recrystallized from ether-ethanol and dried at room temperature to yield 80.2 g of 3-amino-1-(2-furanyl)-2-buten-1-one, m.p. 128°-130° C. Another 33.4 g of the product, m.p. 128°-130° C. was collected by concentrating the mother liquor and extracting the product with ether.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04650806
출처 데이터셋uspto-grants-1987_03
ORD IDord-1c1a73a4389c4affa6a806ad68320814
출처 메모uspto-grants-1987_03